Methods and compositions for diagnosis and prognosis of renal artery stenosis

ABSTRACT

The present invention relates to methods and compositions for monitoring, diagnosis, prognosis, and determination of treatment regimens in subjects in the context of renal artery stenosis (RAS). In particular, the invention relates to using assays that detect NGAL, their use to diagnose RAS in subjects suffering from hypertension, and their use in prognosis, particularly of mortality and worsening renal function.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is filed pursuant to 35 U.S.C. §371 as a United States National Phase Application of International Application No. PCT/US2007/084700, filed Nov. 14, 2007, which claims benefit under 35 U.S.C. §119(e) of U.S. Application No. 60/859,136 filed Nov. 14, 2006, each of which is incorporated herein by reference in its entirerty.

FIELD OF THE INVENTION

The present invention relates to methods and compositions for monitoring renal artery stenosis.

BACKGROUND OF THE INVENTION

The following discussion of the background of the invention is merely provided to aid the reader in understanding the invention and is not admitted to describe or constitute prior art to the present invention.

Patients with hypertension have some underlying mechanism that elevates their blood pressure. This hypertension can be generally separated into one of two classes: essential hypertension (systemic hypertension of unknown cause); and secondary hypertension (hypertension that results from an underlying, identifiable, often correctable cause). Renal artery stenosis (RAS) is one of the main causes of secondary systemic arterial hypertension. Depending on the severity of the disease, the ultimate clinical consequences (hypertension and renal failure) can lead to mortality at an alarming rate. For example, the reported cumulative two year survival rate for patients diagnosed with unilateral renal artery stenosis is 96%, for bilateral stenosis 74%, and for bilateral stenosis with one or both renal arteries occluded it is 47%. Atherosclerosis accounts for 90% of cases of RAS, and usually involves the ostium and the proximal segment of the main renal artery and the perirenal aorta, with fibromuscular dysplasia accounting for the majority of the remaining cases.

Atherosclerotic RAS is a common and progressive disease. Its prevalence increases with age, particularly in patients who have diabetes, aortoiliac occlusive disease, coronary artery disease or hypertension. Available treatments include percutaneous transluminal angioplasty, endovascular stent placement or surgical revascularization. Doppler ultrasound, magnetic resonance angiography, and computed tomographic angiography has been used to screen for suspected renovascular disease in patients at risk for RAS.

BRIEF SUMMARY OF THE INVENTION

It is an object of the invention to provide methods and compositions for diagnosis, prognosis, and determination of further diagnosis and treatment regimens in subjects suffering or at risk of suffering from renal artery stenosis. Using an early marker of renal dysfunction such as NGAL (also known as neutrophil gelatinase-associated lipocalin, human precursor Swiss-Prot P80188), subjects at risk for poor outcomes due to previously undiagnosed RAS can be identified, and subjects previously diagnosed as having RAS can be monitored for early signs of worsening renal function and/or increased mortality risk. In addition, subjects that could benefit from additional diagnostics, such as Doppler ultrasound, magnetic resonance angiography, and computed tomographic angiography, or therapies such as percutaneous transluminal angioplasty, endovascular stent placement or surgical revascularization can be readily identified.

In a first aspect, the present invention relates to methods for diagnosing renal artery stenosis in a subject suffering from hypertension. These methods comprise performing an assay method that configured to detect NGAL (and/or one or more markers related thereto, as that term is defined herein) on a body fluid sample obtained from such a subject suffering. The assay result (referred to herein as an “NGAL assay result,” which may be expressed in the form of an NGAL concentration) is compared to a baseline NGAL result, and a diagnosis of renal artery stenosis is assigned to the subject when the NGAL assay result is above the baseline. In the alternative, a diagnosis of renal artery stenosis is ruled out for the subject when the NGAL assay result is below the baseline.

A variety of methods may be used by the skilled artisan to arrive at a desired baseline. In certain embodiments, the baseline NGAL result is determined from a population of subjects suffering from hypertension, most preferably from renovascular hypertension, and is based on an NGAL result that can provide an acceptable level of specificity and sensitivity in separating the population into a “first” subpopulation having an increased likelihood of renal artery stenosis relative to the remaining “second” subpopulation. As discussed herein, a preferred baseline NGAL result separates this first and second population by one or more of the following measures of test accuracy:

-   an odds ratio of at least about 2 or more or about 0.5 or less, more     preferably at least about 3 or more or about 0.33 or less, still     more preferably at least about 4 or more or about 0.25 or less, even     more preferably at least about 5 or more or about 0.2 or less, and     most preferably at least about 10 or more or about 0.1 or less. -   at least 75% sensitivity, combined with at least 75% specificity; -   a ROC curve area of at least 0.6, more preferably 0.7, still more     preferably at least 0.8, even more preferably at least 0.9, and most     preferably at least 0.95; and/or -   a positive likelihood ratio (calculated as     sensitivity/(1-specificity)) of at least 5, more preferably at least     10, and most preferably at least 20; or -   a negative likelihood ratio (calculated as     (1-sensitivity)/specificity) of less than or equal to 0.3, more     preferably less than or equal to 0.2, and most preferably less than     or equal to 0.1. The term “about” in this context refers to +/−5% of     a given measurement.

Preferred assay methods comprise performing an immunoassay that detects NGAL. Antibodies for use in such assays will specifically bind NGAL, and may optionally also bind one or more polypeptides that are “related” thereto, as described hereinafter with regard to related markers. Such immunoassays may comprise contacting said body fluid sample with a solid phase comprising antibody that detects NGAL, and detecting binding to said antibody, although assay formats that do not require the use of a solid phase are known in the art. Preferably, the body fluid sample is selected from the group consisting of urine, blood, serum, and plasma.

In addition to NGAL assay results, additional variables may be included in the methods for diagnosing renal artery stenosis described herein. As described in additional detail hereinafter, additional diagnostics, such as Doppler ultrasound, magnetic resonance angiography, and computed tomographic angiography, may be performed, and the diagnosis can be based on both the NGAL assay result and the results of these other diagnostics. For example, a diagnosis of renal artery stenosis may be assigned to the subject when the NGAL assay result is above the baseline and when confirmed by one of these other diagnostic methods.

In another aspect, the present invention relates to methods for assigning a risk of one or more adverse outcomes, such as future risk of mortality and/or a future risk of worsening renal function, to a patient suffering from renal artery stenosis. These methods comprise performing an assay method that configured to detect NGAL (and/or one or more markers related thereto, as that term is defined herein) on a body fluid sample obtained from such a subject. The assay result (referred to herein as an “NGAL assay result,” which may be expressed in the form of an NGAL concentration) is compared to a baseline NGAL result, and an increased risk of one or more adverse outcomes is assigned to the subject when the NGAL assay result is above the baseline, relative to a risk assigned when the NGAL assay result is below the baseline. In the alternative, a decreased risk of one or more adverse outcomes is assigned to the subject when the NGAL assay result is below the baseline, relative to a risk assigned when the NGAL assay result is above than the baseline.

As discussed herein, a variety of methods may be used by the skilled artisan to arrive at a desired baseline. In certain preferred embodiments, the baseline NGAL result is determined from an earlier NGAL assay result obtained from the same subject. That is, the change in NGAL concentration may be observed over time, and an increased NGAL concentration provides an indication of worsening renal function, an increased risk of mortality, etc., in the patient.

In alternative embodiments, the baseline NGAL result is determined from a population of subjects in which outcome has been followed, and is based on an NGAL result that can provide an acceptable level of specificity and sensitivity in separating the population into a “first” subpopulation having an increased (or decreased) risk of one or more adverse outcomes relative to the remaining “second” subpopulation. A preferred baseline NGAL result separates this first and second population by one or more of the following measures of test accuracy:

-   an odds ratio of at least about 2 or more or about 0.5 or less, more     preferably at least about 3 or more or about 0.33 or less, still     more preferably at least about 4 or more or about 0.25 or less, even     more preferably at least about 5 or more or about 0.2 or less, and     most preferably at least about 10 or more or about 0.1 or less. -   at least 75% sensitivity, combined with at least 75% specificity; -   a ROC curve area of at least 0.6, more preferably 0.7, still more     preferably at least 0.8, even more preferably at least 0.9, and most     preferably at least 0.95; and/or -   a positive likelihood ratio (calculated as     sensitivity/(1-specificity)) of at least 5, more preferably at least     10, and most preferably at least 20; or -   a negative likelihood ratio (calculated as     (1-sensitivity)/specificity) of less than or equal to 0.3, more     preferably less than or equal to 0.2, and most preferably less than     or equal to 0.1. The term “about” in this context refers to +/−5% of     a given measurement.

The present methods preferably assign a “near-term” risk of one or more adverse outcomes. By “near term” is meant within 30 days. As described hereinafter, the methods preferably assign a risk of one or more adverse outcomes within 7 days, more preferably within 5 days, and still more preferably within 3 days.

As is also described above, preferred assay methods comprise performing an immunoassay that detects NGAL. Antibodies for use in such assays can specifically bind NGAL, and may optionally also bind one or more polypeptides that are “related” thereto. Such immunoassays may comprise contacting said body fluid sample with a solid phase comprising antibody that detects NGAL, and detecting binding to said antibody, although assay formats that do not require the use of a solid phase are known in the art. Preferably, the body fluid sample is selected from the group consisting of urine, blood, serum, and plasma.

In addition to NGAL assay results, additional variables may be included in the methods for assigning a mortality risk in the context of renal dysfunction. As described in additional detail hereinafter, assays that detect various markers (both subject-derived and physical characteristics) may be combined, including assays that detect various natriuretic peptides such as BNP, NT-proBNP, and proBNP; markers related to inflammation such as myeloperoxidase, soluble FLT-1, C-reactive protein, and placental growth factor; markers related to cardiac damage such as cardiac troponins and CK-MB; markers of renal damage such as serum creatinine, creatinine clearance rates, cystatin C, and glomerular filtration rates; and variables such as urine output levels, age, the presence or absence of various cardiovascular risk factors such as diabetes, hypertension, body mass, smoking status, etc. In these “multiple marker” methods, the patient's mortality risk is assigned based both on comparing the NGAL assay result to the baseline NGAL result as described above, and on one or more of these additional variables. In many cases, these additional variables can be used in a manner analogous to NGAL, in that baseline results can be established for these markers as described herein for comparison of a test result measured on a body fluid sample. In other cases, such as sex, cardiovascular risk factors, etc., the variables can be dichotomized for analysis of risk. For example, different NGAL baselines may be established for different age groups, and/or based on sex of the subject.

As noted above, the various assays can be performed on the same or different body fluid samples. For example, NGAL may be measured in a urine sample and BNP may be measured in a plasma sample; or NGAL may be measured in a plasma sample and cystatin C measured in a different plasma sample.

In still another aspect, the present invention relates to methods for assigning a patient to a diagnostic pathway. These methods comprise performing an assay method that configured to detect NGAL (and/or one or more markers related thereto, as that term is defined herein) on a body fluid sample obtained from such a subject. The assay result (referred to herein as an “NGAL assay result,” which may be expressed in the form of an NGAL concentration) is compared to a baseline NGAL result, and a subject is assigned to receive additional diagnostic tests for identification of renal artery stenosis when the NGAL assay result is above the baseline.

In a related aspect, the present invention relates to methods for assigning a patient to a therapeutic pathway. These methods comprise performing an assay method that configured to detect NGAL (and/or one or more markers related thereto, as that term is defined herein) on a body fluid sample obtained from such a subject. The assay result (referred to herein as an “NGAL assay result,” which may be expressed in the form of an NGAL concentration) is compared to a baseline NGAL result, and a subject is assigned to receive therapy for renal artery stenosis when the NGAL assay result is above the baseline.

As in the previous aspects, a variety of methods may be used by the skilled artisan to arrive at a desired baseline value. In certain embodiments, the baseline NGAL result is determined from a population of subjects suffering from secondary hypertension, and is based on an NGAL result that can provide an acceptable level of specificity and sensitivity in separating the population into a “first” subpopulation having an increased likelihood of renal artery stenosis relative to the remaining “second” subpopulation.

As discussed herein, a preferred baseline result separates this first and second population by one or more of the following measures of test accuracy:

-   an odds ratio of at least about 2 or more or about 0.5 or less, more     preferably at least about 3 or more or about 0.33 or less, still     more preferably at least about 4 or more or about 0.25 or less, even     more preferably at least about 5 or more or about 0.2 or less, and     most preferably at least about 10 or more or about 0.1 or less. -   at least 75% sensitivity, combined with at least 75% specificity; -   a ROC curve area of at least 0.6, more preferably 0.7, still more     preferably at least 0.8, even more preferably at least 0.9, and most     preferably at least 0.95; and/or -   a positive likelihood ratio (calculated as     sensitivity/(1−specificity)) of at least 5, more preferably at least     10, and most preferably at least 20; or -   a negative likelihood ratio (calculated as     (1−sensitivity)/specificity) of less than or equal to 0.3, more     preferably less than or equal to 0.2, and most preferably less than     or equal to 0.1. The term “about” in this context refers to +/−5% of     a given measurement.

In the case of assigning a subject to a therapeutic pathway, additional variables may be included in the methods for assigning a risk of worsening renal function described herein. For example, additional diagnostics, such as Doppler ultrasound, magnetic resonance angiography, and computed tomographic angiography, may be performed, and therapy can be initiated based on both the NGAL assay result and the results of these other diagnostics. For example, a therapy for renal artery stenosis may be performed on the subject when the NGAL assay result is above the baseline and when confirmed by one of these other diagnostic methods.

Preferred therapy pathways comprise performing one or more of percutaneous transluminal angioplasty, endovascular stent placement or surgical revascularization on the subject.

In various related aspects, the present invention relates to devices and kits for performing the methods described herein. Suitable kits comprise reagents sufficient for performing at least one of the described NGAL assays, together with instructions for performing the described baseline comparisons. In certain embodiments, reagents for performing such assays are provided in an assay device, and such assay devices may be included in such a kit. Preferred reagents comprise one or more solid phase antibodies, the solid phase antibody comprising antibody that detects the intended target(s) bound to a solid support. In the case of sandwich immunoassays, such reagents can also include one or more detectably labeled antibodies, the detectably labeled antibody comprising antibody that detects the intended target(s) bound to a detectable label. Additional optional elements that may be provided as part of an assay device are described hereinafter.

DETAILED DESCRIPTION OF THE INVENTION

The present invention relates to methods and compositions for diagnosis, prognosis, and determination of treatment regimens in subjects suffering from or at risk of suffering from renal artery stenosis.

The term “hypertension” refers to blood pressure that is elevated above normal levels (e.g., a systolic blood pressure ≧140 mm Hg and/or a diastolic blood pressure ≧90 mm Hg) or a subject taking antihypertensive medication. Between 85 and 90% of hypertensives have primary hypertension, which is typically of unknown etiology. A discussion of the numerous factors believed involved in primary hypertension, diagnostic methods, treatments, etc., is provided in The Merck Manual of Diagnosis and Therapy, 17^(th) Ed., Merck & Co., Inc., 1999, pages 1629-1648.

In contrast, renovascular hypertension accounts for less than 2% of all cases of hypertension. The term “renovascular hypertension” as used herein refers to acute or chronic elevation of blood pressure caused by complete or partial occlusion of one or more renal arteries or their branches. This complete or partial occlusion is referred to herein as “renal artery stenosis.” It has been reported that the lumen of the stenotic artery must be occluded by at least 70% before changes to systemic blood pressure becomes significant. Thus, the ability to identify such stenosis at an early stage can improve therapy success.

The present invention provides methods and compositions that may be used to monitor renal artery stenosis in patients at risk therefrom. Preferably, a patient is identified as being at risk of renal artery stenosis due to the presence of one or more risk factors of atherosclerosis (e.g., family history of atherosclerosis, obesity, positive smoking status, prior smoking history, race (blacks at an increased risk as compared to whites), >40 years of age plus hypertension, dyslipidemia, diabetes mellitus, etc.). By monitoring NGAL and/or its related markers, an early indication of renal damage that signals renal artery stenosis can be obtained.

The term “renal dysfunction” as used herein refers to a reduced level of kidney function, relative to normal, and is indicated by a serum or plasma creatinine level 1.4 mg/dL or greater, a creatinine clearance rate of 60 mL/min/1.73 m² or less, a serum or plasma cystatin C level of 1 mg/L or greater, or the presence of chronic kidney disease as defined by the National Kidney Foundation in “National Kidney Foundation. Kidney Disease Outcome Quality Initiative (K/DOQI) clinical practice guidelines for chronic kidney disease: evaluation, classification, and stratification,” Am. J. Kidney Dis. 39(Suppl 1):S1-S266, 2002, which is hereby incorporated by reference in its entirety. Chronic kidney disease includes persistent kidney damage, as reflected by a glomerular filtration rate (GFR) of less than 60.0 mL/minute/1.73 m² of body-surface area for more than three months. Included are patients with end-stage renal disease, as defined by a GFR of less than 10.0 mL/minute/1.73 m². Because practical limitations exist in measuring GFR directly, especially in acutely ill patients, clinical variables may be used to estimate the GFR. See, e.g., Levey et al., “A more accurate method to estimate glomerular filtration rate from serum creatinine: a new prediction equation,” Ann. Intern. Med. 130: 461-70, 1999, which is hereby incorporated by reference in its entirety.

Preferred subjects having renal dysfunction are those having severe renal dysfunction (defined herein as serum or plasma creatinine >2.5 mg/dL, serum or plasma cystatin C>2 mg/L, or creatinine clearance rates of <25 mL/minute/1.73 m²), more preferred subjects have moderate renal dysfunction (defined herein as serum or serum or plasma creatinine of 1.9 to 2.5 mg/dL, serum or plasma cystatin C of 2 to 1.5 mg/L, or creatinine clearance rates of 25-30 mL/minute/1.73 m²), and most preferred subjects have mild renal dysfunction (defined herein as serum or plasma creatinine of 1.4 to 2.25 mg/dL, serum or plasma cystatin C of 1 to 1.5 mg/L, or creatinine clearance rates of 30-60 mL/minute/1.73 m²).

The term “risk of worsening renal function” as used herein refers to assignment of a particular prognosis—a likelihood that a subject will suffer, most preferably in the short term, from deterioration of one or more measures of kidney function selected from the group consisting of serum or plasma creatinine levels, creatinine clearance rates, serum or plasma cystatin C levels, chronic kidney disease stage (as defined by the National Kidney Foundation in “National Kidney Foundation. Kidney Disease Outcome Quality Initiative (K/DOQI) clinical practice guidelines for chronic kidney disease: evaluation, classification, and stratification,” Am. J. Kidney Dis. 39(Suppl 1): S1-S266, 2002), stage of renal dysfunction, and glomerular filtration rate, or, in the extreme, will die (that is, a likelihood of mortality in the subject).

As described herein, the present invention relates in part to assigning a risk of an adverse outcome (e.g., worsening renal function or mortality) based, at least in part, on the result of an assay that detects NGAL performed on a body fluid sample obtained from a subject suffering from renal artery stenosis. If the sample tested is obtained from the subject at a time t, the phrase “the short term” refers to a 7-day (168 hour) period measured from time t. Thus, the risk is a likelihood that the subject will suffer from such an adverse outcome, in a window beginning at time t and ending 168 hours later. More preferably, the risk is a likelihood that the subject will suffer from deterioration of one or more of these measures of kidney function, or will die, in a 96 hour window beginning at time t, and most preferably the risk is a likelihood that the subject will suffer from deterioration of one or more of these measures of kidney function, or a likelihood that the subject will die, in a window of between 48 and 84 hours beginning at time t.

The term “deterioration” as used herein refers to a change in a parameter at a later time, relative to a measure of the same parameter earlier in the same subject, and is the opposite of “improvement.” Thus, the terms “deterioration of serum or plasma creatinine levels” and “deterioration of serum or plasma cystatin C levels” as used herein refer to an increase in the creatinine or cystatin C assay result in a sample obtained from a subject at a time later than time t, relative to that measured in the subject at time t. Similarly, “deterioration of creatinine clearance rates” as used herein refers to a later decrease in creatinine clearance rate for the subject, relative to that measured at time t. “Deterioration in chronic kidney disease stage” as used herein refers to a later change to a higher stage in the subject, relative to that observed at time t. “Deterioration of stage of renal dysfunction” as used herein refers to a later change in the subject from mild to moderate or severe, or a change from moderate to severe, relative to the stage of renal dysfunction observed at time t. Finally, “deterioration of glomerular filtration rate” as used herein refers to a later decrease in GFR in the subject, relative to that observed at time t.

The term “marker” as used herein refers to proteins, polypeptides, glycoproteins, proteoglycans, lipids, lipoproteins, glycolipids, phospholipids, nucleic acids, carbohydrates, etc. or small molecules to be used as targets for screening test samples obtained from subjects. “Proteins or polypeptides” used as markers in the present invention are contemplated to include any fragments thereof, in particular, immunologically detectable fragments. Markers can also include clinical “scores” such as a systolic and/or diastolic blood pressure, pre-test probability assignment, a pulmonary hypertension “Daniel” score, an NIH stroke score, a Sepsis Score of Elebute and Stoner, a Duke Criteria for Infective Endocarditis, a Mannheim Peritonitis Index, an “Apache” score, etc.

The term “related marker” as used herein refers to one or more fragments of a particular marker or its biosynthetic parent that may be detected as a surrogate for the marker itself or as independent markers. By way of example, human BNP is derived by proteolysis of a 108 amino acid precursor molecule, referred to hereinafter as BNP₁₋₁₀₈. Mature BNP, or “the BNP natriuretic peptide,” or “BNP-32” is a 32 amino acid molecule representing amino acids 77-108 of this precursor, which may be referred to as BNP₇₇₋₁₀₈. The remaining residues 1-76 are referred to hereinafter as BNP₁₋₇₆, and are also known as “NT-proBNP.” Additionally, related markers may be the result of covalent modification of the parent marker, for example by oxidation of methionine residues, ubiquitination, cysteinylation, nitrosylation (e.g., containing nitrotyrosine residues), halogenation (e.g., containing chlorotyrosine and/or bromotyrosine residues), glycosylation, complex formation, differential splicing, etc. Preferred related markers are “immunologically detectable,” meaning a fragment of a particular marker or its biosynthetic parent that comprises at least one epitope (antigenic site on the polypeptide to which an antibody binds) that is also present in the marker or its biosynthetic parent. Preferred immunologically detectable fragments comprise at least 8 contiguous residues of the marker or its biosynthetic parent.

While mature BNP itself may be used as a marker in the present invention, the prepro-BNP, BNP₁₋₁₀₈ and BNP₁₋₇₆ molecules represent BNP-related markers that may be measured either as surrogates for mature BNP or as markers in and of themselves. In addition, one or more fragments of these molecules may also be present in circulation. Moreover, assays may intentionally use proteolysis to generate fragments of a marker, which may then be measured. See, e.g., Goetze et al., “Quantification of pro-B-type natriuretic peptide and its products in human plasma by use of an analysis independent of precursor processing,” Clin. Chem. 48: 1035-42, 2002. “Related markers” to NGAL may be identified and used in an analogous fashion to that described above for BNP.

Because production of marker fragments is an ongoing process that may be a function of, inter alia, the elapsed time between onset of an event triggering marker release into the tissues and the time the sample is obtained or analyzed; the elapsed time between sample acquisition and the time the sample is analyzed; the type of tissue sample at issue; the storage conditions; the quantity of proteolytic enzymes present; etc., it may be necessary to consider this degradation when both designing an assay for one or more markers, and when performing such an assay, in order to provide an accurate prognostic or diagnostic result. In addition, individual antibodies that distinguish amongst a plurality of marker fragments may be individually employed to separately detect the presence or amount of different fragments. The results of this individual detection may provide a more accurate prognostic or diagnostic result than detecting the plurality of fragments in a single assay. For example, different weighting factors may be applied to the various fragment measurements to provide a more accurate estimate of the amount of natriuretic peptide originally present in the sample.

Preferred assays are “configured to detect” a particular marker. That an assay is “configured to detect” a marker means that an assay can generate a detectable signal indicative of the presence or amount of a physiologically relevant concentration of a particular marker of interest. Such an assay may, but need not, specifically detect a particular marker (i.e., detect a marker but not some or all related markers). Because an antibody epitope is on the order of 8 amino acids, an immunoassay will detect other polypeptides (e.g., related markers) so long as the other polypeptides contain the epitope(s) necessary to bind to the antibody used in the assay. Such other polypeptides are referred to as being “immunologically detectable” in the assay, and would include various isoforms (e.g., splice variants). In the case of a sandwich immunoassay, related markers must contain at least the two epitopes bound by the antibody used in the assay in order to be detected.

The methods described hereinafter utilize assays that detect NGAL, and/or its related markers. Such markers are referred to herein as being “subject-derived.” The term “subject-derived marker” as used herein refers to protein, polypeptide, phospholipid, nucleic acid, prion, glycoprotein, proteoglycan, glycolipid, lipid, lipoprotein, carbohydrate, or small molecule markers that are expressed or produced by one or more cells of the subject. Additional markers may be used that are derived not from the subject, but rather that are expressed by pathogenic or infectious organisms that are correlated with a particular disease. Such markers are preferably protein, polypeptide, phospholipid, nucleic acid, prion, or small molecule markers that identify the infectious diseases described above. These subject-derived markers are measured in a test sample, most preferably a body fluid sample.

The term “test sample” as used herein refers to a sample of bodily fluid obtained for the purpose of diagnosis, prognosis, or evaluation of a subject of interest, such as a patient. In certain embodiments, such a sample may be obtained for the purpose of determining the outcome of an ongoing condition or the effect of a treatment regimen on a condition. Preferred test samples include blood, serum, plasma, cerebrospinal fluid, urine, saliva, sputum, and pleural effusions. In addition, one of skill in the art would realize that some test samples would be more readily analyzed following a fractionation or purification procedure, for example, separation of whole blood into serum or plasma components.

As used herein, a “plurality” as used herein refers to at least two. Preferably, a plurality refers to at least 3, more preferably at least 5, even more preferably at least 10, even more preferably at least 15, and most preferably at least 20. In particularly preferred embodiments, a plurality is a large number, i.e., at least 100.

The term “subject” as used herein refers to a human or non-human organism. Thus, the methods and compositions described herein are applicable to both human and veterinary disease. Further, while a subject is preferably a living organism, the invention described herein may be used in post-mortem analysis as well. Preferred subjects are “patients,” i.e., living humans that are receiving medical care for a disease or condition. This includes persons with no defined illness who are being investigated for signs of pathology.

The term “diagnosis” as used herein refers to methods by which the skilled artisan can estimate and/or determine whether or not a patient is suffering from a given disease or condition. The skilled artisan often makes a diagnosis on the basis of one or more diagnostic indicators, i.e., a marker, the presence, absence, amount, or change in amount of which is indicative of the presence, severity, or absence of the condition. The term “diagnosis” does not refer to the ability to determine the presence or absence of a particular disease with 100% accuracy, or even that a given course or outcome is more likely to occur than not. Instead, the skilled artisan will understand that the term “diagnosis” refers to an increased probability that a certain disease is present in the subject.

Similarly, a prognosis is often determined by examining one or more “prognostic indicators.” These are markers, the presence or amount of which in a patient (or a sample obtained from the patient) signal a probability that a given course or outcome will occur. For example, when one or more prognostic indicators reach a sufficiently high level in samples obtained from such patients, the level may signal that the patient is at an increased probability for experiencing morbidity or mortality in comparison to a similar patient exhibiting a lower marker level. A level or a change in level of a prognostic indicator, which in turn is associated with an increased probability of morbidity or death, is referred to as being “associated with an increased predisposition to an adverse outcome” in a patient.

The term “correlating” or “relating” as used herein in reference to the use of markers, refers to comparing the presence or amount of the marker(s) in a patient to its presence or amount in persons known to suffer from, or known to be at risk of, a given condition; or in persons known to be free of a given condition. As discussed above, a marker level in a patient sample can be compared to a level known to be associated with a specific diagnosis. The sample's marker level is said to have been correlated with a diagnosis; that is, the skilled artisan can use the marker level to determine whether the patient suffers from a specific type diagnosis, and respond accordingly. Alternatively, the sample's marker level can be compared to a marker level known to be associated with a good outcome (e.g., the absence of disease, etc.). In preferred embodiments, a profile of marker levels are correlated to a global probability or a particular outcome using ROC curves.

In certain embodiments, the methods described herein comprise the comparison of an assay result to a corresponding baseline result. The term “baseline result” as used herein refers to an assay value that is used as a comparison value (that is, to which a test result is compared). In practical terms, this means that a marker is measured in a sample from a subject, and the result is compared to the baseline result. A value above the baseline indicates a first likelihood of a diagnosis or prognosis, and a value below the baseline indicates a second likelihood of a diagnosis or prognosis.

In certain embodiments, a baseline for NGAL (and/or one or more markers related thereto) is established, and an NGAL assay result is established by performing an assay method that detects NGAL on a sample from a patient suffering from hypertension. That NGAL result is compared to the NGAL baseline result, and a value above the baseline indicates an increased likelihood of renal artery stenosis, relative to a value below the baseline. Similarly, a value below the baseline indicates a decreased likelihood of renal artery stenosis, relative to a value above the baseline. Such a comparison is said to be “diagnostic” of renal artery stenosis.

In other embodiments, a baseline for NGAL (and/or one or more markers related thereto) is established, and an NGAL assay result is established by performing an assay method that detects NGAL on a sample from a patient diagnosed as having renal artery stenosis. That NGAL result is compared to the NGAL baseline result, and a value above the baseline indicates an increased risk of an adverse outcome, relative to risk assigned to a value below the baseline. Similarly, a value below the baseline indicates a decreased risk of an adverse outcome, relative to a value above the baseline. Preferred methods predict a risk of worsening renal function and/or death. Such a comparison is said to be “prognostic” of potential outcomes of renal artery stenosis

In yet other embodiments, a baseline for NGAL (and/or one or more markers related thereto) is established, and an NGAL assay result is established by performing an assay method that detects NGAL on a sample from a patient, preferably selected for being at risk of renal artery stenosis or for suffering from hypertension. That NGAL result is compared to the NGAL baseline result, and a value above the baseline indicates that the patient should be sent for further evaluation of renal artery stenosis, for example by performing imaging studies known in the art.

In still other embodiments, a baseline for NGAL (and/or one or more markers related thereto) is established, and an NGAL assay result is established by performing an assay method that detects NGAL on a sample from a patient. That NGAL result is compared to the NGAL baseline result, and a value above the baseline indicates that the patient should be sent for therapy for renal artery stenosis.

A baseline can be selected in a number of manners well known to those of skill in the art. For example, data for a marker or markers (e.g., concentration in a body fluid, such as urine, blood, serum, or plasma) may be obtained from a population of subjects. The population of subjects is divided into at least two subpopulations. The first subpopulation includes those subjects who have been confirmed as having a disease, outcome, or, more generally, being in a first condition state. For example, this first subpopulation of patients may be those diagnosed with hypertension, and that are diagnosed with renal artery stenosis as a cause of that hypertension. For convenience, subjects in this first subpopulation will be referred to as “diseased,” although in fact, this subpopulation is actually selected for the presence of a particular characteristic of interest. The second subpopulation of subjects is formed from the subjects that do not fall within the first subpopulation, for example, those diagnosed with hypertension, and for whom renal artery stenosis has been ruled out as a cause of that hypertension. Subjects in this second set will hereinafter be referred to as “non-diseased.”

In another example, this first subpopulation of patients may be those diagnosed with renal artery stenosis, and that subsequently experience an adverse outcome of their renovascular disease. The second subpopulation of subjects is formed from the subjects that do not fall within the first subpopulation, for example, diagnosed with renal artery stenosis, and that subsequently do not experience the adverse outcome under study.

A baseline result may then be selected to distinguish between the diseased and non-diseased subpopulation with an acceptable specificity and sensitivity. Changing the baseline merely trades off between the number of false positives and the number of false negatives resulting from the use of the particular marker under study. The effectiveness of a test having such an overlap is often expressed using a ROC (Receiver Operating Characteristic) curve. ROC curves are well known to those skilled in the art. The horizontal axis of the ROC curve represents (1-specificity), which increases with the rate of false positives. The vertical axis of the curve represents sensitivity, which increases with the rate of true positives. Thus, for a particular cutoff selected, the value of (1-specificity) may be determined, and a corresponding sensitivity may be obtained. The area under the ROC curve is a measure of the probability that the measured marker level will allow correct identification of a disease or condition. Thus, the area under the ROC curve can be used to determine the effectiveness of the test.

In an alternative, an individual subject may provide their own baseline, in that a temporal change is used to indicate a particular diagnosis or prognosis. For example, one or more markers may be determined at an initial time to provide one or more baseline results, and then again at a later time, and the change (or lack thereof) in the marker level(s) over time determined. In such embodiments, an increase in the marker from the initial time to the second time may be indicative of a particular prognosis, of a particular diagnosis, etc. Likewise, a decrease in the marker from the initial time to the second time may be indicative of a particular prognosis, of a particular diagnosis, etc. In such an embodiment, a plurality of markers need not change in concert with one another. Temporal changes in one or more markers may also be used together with single time point marker levels compared to a population-based baseline.

As discussed herein, the measurement of the level of a single marker such as NGAL may be augmented by additional markers. For example, other markers related to blood pressure regulation, including other natriuretic peptides and/or their related markers may be used together with, or separately from, BNP and/or its related markers. Suitable assays include, but are not limited to, assays that detect ANP, proANP, NT-proANP, CNP, Kininogen, CGRP II, urotensin II, BNP, NT-proBNP, proBNP, calcitonin gene related peptide, arg-Vasopressin, Endothelin-1 (and/or Big ET-1), Endothelin-2 (and/or Big ET-2), Endothelin-3 (and/or Big ET-3), procalcitonin, calcyphosine, adrenomedullin, aldosterone, angiotensin 1 (and/or angiotensinogen 1), angiotensin 2 (and/or angiotensinogen 2), angiotensin 3 (and/or angiotensinogen 3), Bradykinin, Tachykinin-3, calcitonin, Renin, Urodilatin, and Ghrelin, and/or one or more markers related thereto. Preferred assays detect marker(s) selected from the group consisting of BNP, NT-proBNP, and proBNP.

Other markers of renal function may also be used in the methods described herein. These include serum creatinine levels, creatinine clearance rates, cystatin C levels, and glomerular filtration rates.

In addition, subjects suffering from renovascular are often at increased risk for cardiovascular diseases, including potentially fatal arrhythmias and acute coronary syndromes. Thus, various subject-derived markers of cardiovascular risk may be included together with NGAL (and/or its related markers). Suitable subject-derived markers include markers related to myocardial injury, markers related to coagulation and hemostasis, and markers related to inflammation. In addition, because of injury to pulmonary tissues occurring in heart failure, various markers related to pulmonary injury may also be included. Exemplary subject-derived markers are provided in the following table:

Marker Classification Neutrophil elastase Pulmonary injury KL-6 Pulmonary injury LAMP 3 Pulmonary injury LAMP3 Pulmonary injury Lung Surfactant protein A Pulmonary injury Lung Surfactant protein B Pulmonary injury Lung Surfactant protein C Pulmonary injury Lung Surfactant protein D Pulmonary injury phospholipase D Pulmonary injury PLA2G5 Pulmonary injury SFTPC Pulmonary injury Myoglobin Tissue injury E-selectin Tissue injury VEGF Tissue injury EG-VEGF Tissue injury Troponin I and complexes Myocardial injury Troponin T and complexes Myocardial injury Annexin V Myocardial injury B-enolase Myocardial injury CK-MB Myocardial injury Glycogen phosphorylase-BB Myocardial injury Heart type fatty acid binding protein Myocardial injury Phosphoglyceric acid mutase Myocardial injury S-100ao Myocardial injury Plasmin Coagulation and hemostasis Thrombin Coagulation and hemostasis Antithrombin-III Coagulation and hemostasis Fibrinogen Coagulation and hemostasis von Willebrand factor Coagulation and hemostasis D-dimer Coagulation and hemostasis PAI-1 Coagulation and hemostasis Protein C Coagulation and hemostasis Soluble Endothelial Protein C Receptor Coagulation and hemostasis (EPCR) TAFI Coagulation and hemostasis Fibrinopeptide A Coagulation and hemostasis Plasmin alpha 2 antiplasmin complex Coagulation and hemostasis Platelet factor 4 Coagulation and hemostasis Platelet-derived growth factor Coagulation and hemostasis P-selectin Coagulation and hemostasis Prothrombin fragment 1 + 2 Coagulation and hemostasis B-thromboglobulin Coagulation and hemostasis Thrombin antithrombin III complex Coagulation and hemostasis Thrombomodulin Coagulation and hemostasis Thrombus Precursor Protein Coagulation and hemostasis Tissue factor Coagulation and hemostasis Tissue factor pathway inhibitor-α Coagulation and hemostasis Tissue factor pathway inhibitor-β Coagulation and hemostasis APRIL (TNF ligand superfamily member 13) Inflammatory CD27 (TNFRSF7) Inflammatory Complement C3a Inflammatory CCL-5 (RANTES) Inflammatory CCL-8 (MCP-2) Inflammatory CCL-16 Inflammatory CCL-19 (macrophage inflammatory Inflammatory protein-3β) CCL-20 (MIP-3α) Inflammatory CCL-23 (MIP-3) Inflammatory CXCL-5 (small inducible cytokine B5) Inflammatory CXCL-9 (small inducible cytokine B9) Inflammatory CXCL-13 (small inducible cytokine B13) Inflammatory CXCL-16 (small inducible cytokine B16) Inflammatory DPP-II (dipeptidyl peptidase II) Inflammatory DPP-IV (dipeptidyl peptidase IV) Inflammatory Glutathione S Transferase Inflammatory HIF 1 ALPHA Inflammatory IL-25 Inflammatory IL-23 Inflammatory IL-22 Inflammatory IL-18 Inflammatory IL-13 Inflammatory IL-12 Inflammatory IL-10 Inflammatory IL-1-Beta Inflammatory IL-1ra Inflammatory IL-4 Inflammatory IL-6 Inflammatory IL-8 Inflammatory Lysophosphatidic acid Inflammatory MDA-modified LDL Inflammatory Human neutrophil elastase Inflammatory C-reactive protein Inflammatory Insulin-like growth factor Inflammatory Inducible nitric oxide synthase Inflammatory Intracellular adhesion molecule Inflammatory Lactate dehydrogenase Inflammatory MCP-1 Inflammatory MMP-1 Inflammatory MMP-2 Inflammatory MMP-3 Inflammatory MMP-7 Inflammatory MMP-9 Inflammatory TIMP-1 Inflammatory TIMP-2 Inflammatory TIMP-3 Inflammatory NGAL Inflammatory n-acetyl aspartate Inflammatory PTEN Inflammatory Phospholipase A2 Inflammatory TNF Receptor Superfamily Member 1A Inflammatory TNFRSF3 (lymphotoxin β receptor) Inflammatory Transforming growth factor beta Inflammatory TREM-1 Inflammatory TREM-1sv Inflammatory TL-1 (TNF ligand related molecule-1) Inflammatory TL-1a Inflammatory Tumor necrosis factor alpha Inflammatory Vascular cell adhesion molecule Inflammatory Vascular endothelial growth factor Inflammatory cystatin C Inflammatory substance P Inflammatory Myeloperoxidase (MPO) Inflammatory macrophage inhibitory factor Inflammatory Fibronectin Inflammatory cardiotrophin 1 Inflammatory Haptoglobin Inflammatory PAPPA Inflammatory s-CD40 ligand Inflammatory HMG-1 (or HMGB1) Inflammatory IL-2 Inflammatory IL-4 Inflammatory IL-11 Inflammatory IL-13 Inflammatory IL-18 Inflammatory Eosinophil cationic protein Inflammatory Mast cell tryptase Inflammatory VCAM Inflammatory sICAM-1 Inflammatory TNFα Inflammatory Osteoprotegerin Inflammatory Prostaglandin D-synthase Inflammatory Prostaglandin E2 Inflammatory RANK ligand Inflammatory RANK (TNFRSF11A) Inflammatory HSP-60 Inflammatory Serum Amyloid A Inflammatory s-iL 18 receptor Inflammatory S-iL-1 receptor Inflammatory s-TNFR1 (P55) Inflammatory s-TNFR2 (P75) Inflammatory sTLR-1 (soluble toll-like receptor-1) Inflammatory sTLR-2 Inflammatory sTLR-4 Inflammatory TGF-beta Inflammatory MMP-11 Inflammatory Beta NGF Inflammatory CD44 Inflammatory EGF Inflammatory E-selectin Inflammatory Fibronectin Inflammatory RAGE Inflammatory

Various clinical variables may also be utilized as variables in the methods described herein. Examples of such variables include urine output levels, age, the presence or absence of one or more cardiovascular risk factors such as diabetes, hypertension, smoking status, etc. This list is not meant to be limiting.

Suitable methods for combining markers into a single composite value that may be used as if it is a single marker are described in detail in U.S. Provisional Patent Application No. 60/436,392 filed Dec. 24, 2002, PCT application US03/41426 filed Dec. 23, 2003, U.S. patent application Ser. No. 10/331,127 filed Dec. 27, 2002, and PCT application No. US03/41453, each of which is hereby incorporated by reference in its entirety, including all tables, figures, and claims. In an alternative, NGAL assay results, natriuretic peptide assay results, and other optional test results may be used in an “n-of-m” type of approach. Using a two marker example of such methods, when either marker above its corresponding baseline value may signal an increased risk of an adverse outcome, or a worsening in cardiorenal syndrome status (in n-of-m terms, this is a “1-of-2” result). If both are above the corresponding baselines (a “2-of-2” result), an even greater worsening in cardiorenal syndrome status may be indicated.

The sensitivity and specificity of a diagnostic and/or prognostic test depends on more than just the analytical “quality” of the test—they also depend on the definition of what constitutes an abnormal result. In practice, Receiver Operating Characteristic curves, or “ROC” curves, are typically calculated by plotting the value of a variable versus its relative frequency in “normal” and “disease” populations. For any particular marker, a distribution of marker levels for subjects with and without a “disease” will likely overlap. Under such conditions, a test does not absolutely distinguish normal from disease with 100% accuracy, and the area of overlap indicates where the test cannot distinguish normal from disease. A threshold is selected, above which (or below which, depending on how a marker changes with the disease) the test is considered to be abnormal and below which the test is considered to be normal. The area under the ROC curve is a measure of the probability that the perceived measurement will allow correct identification of a condition. ROC curves can be used even when test results don't necessarily give an accurate number. As long as one can rank results, one can create an ROC curve. For example, results of a test on “disease” samples might be ranked according to degree (say 1=low, 2=normal, and 3=high). This ranking can be correlated to results in the “normal” population, and a ROC curve created. These methods are well known in the art. See, e.g., Hanley et al., Radiology 143: 29-36 (1982).

Measures of test accuracy may also be obtained as described in Fischer et al., Intensive Care Med. 29: 1043-51, 2003, and used to determine the effectiveness of a given marker or panel of markers. These measures include sensitivity and specificity, predictive values, likelihood ratios, diagnostic odds ratios, and ROC curve areas. As discussed above, preferred tests and assays exhibit one or more of the following results on these various measures.

Preferably, a baseline is chosen to exhibit at least about 70% sensitivity, more preferably at least about 80% sensitivity, even more preferably at least about 85% sensitivity, still more preferably at least about 90% sensitivity, and most preferably at least about 95% sensitivity, combined with at least about 70% specificity, more preferably at least about 80% specificity, even more preferably at least about 85% specificity, still more preferably at least about 90% specificity, and most preferably at least about 95% specificity. In particularly preferred embodiments, both the sensitivity and specificity are at least about 75%, more preferably at least about 80%, even more preferably at least about 85%, still more preferably at least about 90%, and most preferably at least about 95%. The term “about” in this context refers to +/−5% of a given measurement.

In other embodiments, a positive likelihood ratio, negative likelihood ratio, odds ratio, or hazard ratio is used as a measure of a test's ability to predict risk or diagnose a disease. In the case of a positive likelihood ratio, a value of 1 indicates that a positive result is equally likely among subjects in both the “diseased” and “control” groups; a value greater than 1 indicates that a positive result is more likely in the diseased group; and a value less than 1 indicates that a positive result is more likely in the control group. In the case of a negative likelihood ratio, a value of 1 indicates that a negative result is equally likely among subjects in both the “diseased” and “control” groups; a value greater than 1 indicates that a negative result is more likely in the test group; and a value less than 1 indicates that a negative result is more likely in the control group. In certain preferred embodiments, markers and/or marker panels are preferably selected to exhibit a positive or negative likelihood ratio of at least about 1.5 or more or about 0.67 or less, more preferably at least about 2 or more or about 0.5 or less, still more preferably at least about 5 or more or about 0.2 or less, even more preferably at least about 10 or more or about 0.1 or less, and most preferably at least about 20 or more or about 0.05 or less. The term “about” in this context refers to +/−5% of a given measurement.

In the case of an odds ratio, a value of 1 indicates that a positive result is equally likely among subjects in both the “diseased” and “control” groups; a value greater than 1 indicates that a positive result is more likely in the diseased group; and a value less than 1 indicates that a positive result is more likely in the control group. In certain preferred embodiments, markers and/or marker panels are preferably selected to exhibit an odds ratio of at least about 2 or more or about 0.5 or less, more preferably at least about 3 or more or about 0.33 or less, still more preferably at least about 4 or more or about 0.25 or less, even more preferably at least about 5 or more or about 0.2 or less, and most preferably at least about 10 or more or about 0.1 or less. The term “about” in this context refers to +/−5% of a given measurement.

In the case of a hazard ratio, a value of 1 indicates that the relative risk of an endpoint (e.g., death) is equal in both the “diseased” and “control” groups; a value greater than 1 indicates that the risk is greater in the diseased group; and a value less than 1 indicates that the risk is greater in the control group. In certain preferred embodiments, markers and/or marker panels are preferably selected to exhibit a hazard ratio of at least about 1.1 or more or about 0.91 or less, more preferably at least about 1.25 or more or about 0.8 or less, still more preferably at least about 1.5 or more or about 0.67 or less, even more preferably at least about 2 or more or about 0.5 or less, and most preferably at least about 2.5 or more or about 0.4 or less. The term “about” in this context refers to +/−5% of a given measurement.

Numerous methods and devices are well known to the skilled artisan for the detection and analysis of the markers of the instant invention. With regard to polypeptides or proteins in patient test samples, immunoassay devices and methods are often used. See, e.g., U.S. Pat. Nos. 6,143,576; 6,113,855; 6,019,944; 5,985,579; 5,947,124; 5,939,272; 5,922,615; 5,885,527; 5,851,776; 5,824,799; 5,679,526; 5,525,524; and 5,480,792, each of which is hereby incorporated by reference in its entirety, including all tables, figures and claims. These devices and methods can utilize labeled molecules in various sandwich, competitive, or non-competitive assay formats, to generate a signal that is related to the presence or amount of an analyte of interest. Additionally, certain methods and devices, such as biosensors and optical immunoassays, may be employed to determine the presence or amount of analytes without the need for a labeled molecule. See, e.g., U.S. Pat. Nos. 5,631,171; and 5,955,377, each of which is hereby incorporated by reference in its entirety, including all tables, figures and claims. One skilled in the art also recognizes that robotic instrumentation including but not limited to Beckman Access, Abbott AxSym, Roche ElecSys, Dade Behring Stratus systems are among the immunoassay analyzers that are capable of performing the immunoassays taught herein.

Preferably the markers are analyzed using an immunoassay, and most preferably sandwich immunoassay, although other methods are well known to those skilled in the art (for example, the measurement of marker RNA levels). The presence or amount of a marker is generally determined using antibodies specific for each marker and detecting specific binding. Any suitable immunoassay may be utilized, for example, enzyme-linked immunoassays (ELISA), radioimmunoassays (RIAs), competitive binding assays, and the like. Specific immunological binding of the antibody to the marker can be detected directly or indirectly. Biological assays such as immunoassays require methods for detection, and one of the most common methods for quantitation of results is to conjugate an enzyme, fluorophore or other molecule to form an antibody-label conjugate. Detectable labels may include molecules that are themselves detectable (e.g., fluorescent moieties, electrochemical labels, metal chelates, etc.) as well as molecules that may be indirectly detected by production of a detectable reaction product (e.g., enzymes such as horseradish peroxidase, alkaline phosphatase, etc.) or by a specific binding molecule which itself may be detectable (e.g., biotin, digoxigenin, maltose, oligohistidine, 2,4-dinitrobenzene, phenylarsenate, ssDNA, dsDNA, etc.). Particularly preferred detectable labels are fluorescent latex particles such as those described in U.S. Pat. Nos. 5,763,189, 6,238,931, and 6,251,687; and International Publication WO95/08772, each of which is hereby incorporated by reference in its entirety. Exemplary conjugation to such particles is described hereinafter. Direct labels include fluorescent or luminescent tags, metals, dyes, radionuclides, and the like, attached to the antibody. Indirect labels include various enzymes well known in the art, such as alkaline phosphatase, horseradish peroxidase and the like.

The use of immobilized antibodies specific for the markers is also contemplated by the present invention. The term “solid phase” as used herein refers to a wide variety of materials including solids, semi-solids, gels, films, membranes, meshes, felts, composites, particles, papers and the like typically used by those of skill in the art to sequester molecules. The solid phase can be non-porous or porous. Suitable solid phases include those developed and/or used as solid phases in solid phase binding assays. See, e.g., chapter 9 of Immunoassay, E. P. Dianiandis and T. K. Christopoulos eds., Academic Press: New York, 1996, hereby incorporated by reference. Examples of suitable solid phases include membrane filters, cellulose-based papers, beads (including polymeric, latex and paramagnetic particles), glass, silicon wafers, microparticles, nanoparticles, TentaGels, AgroGels, PEGA gels, SPOCC gels, and multiple-well plates. See, e.g., Leon et al., Bioorg. Med. Chem. Lett. 8: 2997, 1998; Kessler et al., Agnew. Chem. Int. Ed. 40: 165, 2001; Smith et al., J. Comb. Med. 1: 326, 1999; Orain et al., Tetrahedron Lett. 42: 515, 2001; Papanikos et al., J. Am. Chem. Soc. 123: 2176, 2001; Gottschling et al., Bioorg. Med. Chem. Lett. 11: 2997, 2001. The antibodies could be immobilized onto a variety of solid supports, such as magnetic or chromatographic matrix particles, the surface of an assay place (such as microtiter wells), pieces of a solid substrate material or membrane (such as plastic, nylon, paper), and the like. An assay strip could be prepared by coating the antibody or a plurality of antibodies in an array on solid support. This strip could then be dipped into the test sample and then processed quickly through washes and detection steps to generate a measurable signal, such as a colored spot. When multiple assays are being performed, a plurality of separately addressable locations, each corresponding to a different marker and comprising antibodies that bind the appropriate marker, can be provided on a single solid support. The term “discrete” as used herein refers to areas of a surface that are non-contiguous. That is, two areas are discrete from one another if a border that is not part of either area completely surrounds each of the two areas. The term “independently addressable” as used herein refers to discrete areas of a surface from which a specific signal may be obtained.

For separate or sequential assay of markers, suitable apparatuses include clinical laboratory analyzers such as the ElecSys (Roche), the AxSym (Abbott), the Access (Beckman), the ADVIA® CENTAUR® (Bayer) immunoassay systems, the NICHOLS ADVANTAGE® (Nichols Institute) immunoassay system, etc. Preferred apparatuses perform simultaneous assays of a plurality of markers using a single test device. Particularly useful physical formats comprise surfaces having a plurality of discrete, addressable locations for the detection of a plurality of different analytes. Such formats include protein microarrays, or “protein chips” (see, e.g., Ng and Ilag, J. Cell Mol. Med. 6: 329-340 (2002)) and certain capillary devices (see, e.g., U.S. Pat. No. 6,019,944). In these embodiments, each discrete surface location may comprise antibodies to immobilize one or more analyte(s) (e.g., a marker) for detection at each location. Surfaces may alternatively comprise one or more discrete particles (e.g., microparticles or nanoparticles) immobilized at discrete locations of a surface, where the microparticles comprise antibodies to immobilize one analyte (e.g., a marker) for detection.

Preferred assay devices of the present invention will comprise, for one or more assays, a first antibody conjugated to a solid phase and a second antibody conjugated to a signal development element. Such assay devices are configured to perform a sandwich immunoassay for one or more analytes. These assay devices will preferably further comprise a sample application zone, and a flow path from the sample application zone to a second device region comprising the first antibody conjugated to a solid phase.

Flow of a sample in an assay device along the flow path may be driven passively (e.g., by capillary, hydrostatic, or other forces that do not require further manipulation of the device once sample is applied), actively (e.g., by application of force generated via mechanical pumps, electroosmotic pumps, centrifugal force, increased air pressure, etc.), or by a combination of active and passive driving forces. Most preferably, sample applied to the sample application zone will contact both a first antibody conjugated to a solid phase and a second antibody conjugated to a signal development element along the flow path (sandwich assay format). Additional elements, such as filters to separate plasma or serum from blood, mixing chambers, etc., may be included as required by the artisan. Exemplary devices are described in Chapter 41, entitled “Near Patient Tests: Triage® Cardiac System,” in The Immunoassay Handbook, 2^(nd) ed., David Wild, ed., Nature Publishing Group, 2001, which is hereby incorporated by reference in its entirety.

The analysis of markers could be carried out in a variety of physical formats as well. For example, the use of microtiter plates or automation could be used to facilitate the processing of large numbers of test samples. Alternatively, single sample formats could be developed to facilitate immediate treatment and diagnosis in a timely fashion, for example, in ambulatory transport or emergency room settings.

In another embodiment, the present invention provides a kit for the analysis of markers. Such a kit preferably comprises devises and reagents for the analysis of at least one test sample and instructions for performing the assay(s) of interest. Optionally the kits may contain one or more means for using information obtained from immunoassays performed for a marker panel to rule in or out certain diagnoses or prognoses. Other measurement strategies applicable to the methods described herein include chromatography (e.g., HPLC), mass spectrometry, receptor-based assays, and combinations of the foregoing.

The term “antibody” as used herein refers to a peptide or polypeptide derived from, modeled after or substantially encoded by an immunoglobulin gene or immunoglobulin genes, or fragments thereof, capable of specifically binding an antigen or epitope. See, e.g. Fundamental Immunology, 3^(rd) Edition, W. E. Paul, ed., Raven Press, N.Y. (1993); Wilson (1994) J. Immunol. Methods 175:267-273; Yarmush (1992) J. Biochem. Biophys. Methods 25:85-97. The term antibody includes antigen-binding portions, i.e., “antigen binding sites,” (e.g., fragments, subsequences, complementarity determining regions (CDRs)) that retain capacity to bind antigen, including (i) a Fab fragment, a monovalent fragment consisting of the VL, VH, CL and CH1 domains; (ii) a F(ab′)2 fragment, a bivalent fragment comprising two Fab fragments linked by a disulfide bridge at the hinge region; (iii) a Fd fragment consisting of the VH and CH1 domains; (iv) a Fv fragment consisting of the VL and VH domains of a single arm of an antibody, (v) a dAb fragment (Ward et al., (1989) Nature 341:544-546), which consists of a VH domain; and (vi) an isolated complementarity determining region (CDR). Single chain antibodies are also included by reference in the term “antibody.”

Preferably, an antibody is selected that specifically binds a marker of interest. The term “specifically binds” is not intended to indicate that an antibody binds exclusively to its intended target. Rather, an antibody “specifically binds” if its affinity for its intended target is about 5-fold greater when compared to its affinity for a non-target molecule. Preferably the affinity of the antibody will be at least about 5 fold, preferably 10 fold, more preferably 25-fold, even more preferably 50-fold, and most preferably 100-fold or more, greater for a target molecule than its affinity for a non-target molecule. In preferred embodiments, Specific binding between an antibody or other binding agent and an antigen means a binding affinity of at least 10⁶ M⁻¹. Preferred antibodies bind with affinities of at least about 10⁻¹ M⁻¹, and preferably between about 10⁸ M⁻¹ to about 10⁹ M⁻¹, about 10⁹ M⁻¹ to about 10¹⁰ M⁻¹, or about 10¹⁰ M⁻¹ to about 10⁻¹ M⁻¹.

Affinity is calculated as K_(d)=k_(off)/k_(on) (k_(off) is the dissociation rate constant, k_(on) is the association rate constant and K_(d) is the equilibrium constant. Affinity can be determined at equilibrium by measuring the fraction bound (r) of labeled ligand at various concentrations (c). The data are graphed using the Scatchard equation: r/c=K(n−r):

-   -   where     -   r=moles of bound ligand/mole of receptor at equilibrium;     -   c=free ligand concentration at equilibrium;     -   K=equilibrium association constant; and     -   n=number of ligand binding sites per receptor molecule         By graphical analysis, r/c is plotted on the Y-axis versus r on         the X-axis thus producing a Scatchard plot. The affinity is the         negative slope of the line. k_(off) can be determined by         competing bound labeled ligand with unlabeled excess ligand         (see, e.g., U.S. Pat. No. 6,316,409). The affinity of a         targeting agent for its target molecule is preferably at least         about 1×10⁻⁶ moles/liter, is more preferably at least about         1×10⁻⁷ moles/liter, is even more preferably at least about         1×10⁻⁸ moles/liter, is yet even more preferably at least about         1×10⁻⁹ moles/liter, and is most preferably at least about         1×10⁻¹⁰ moles/liter. Antibody affinity measurement by Scatchard         analysis is well known in the art. See, e.g., van Erp et al., J.         Immunoassay 12: 425-43, 1991; Nelson and Griswold, Comput.         Methods Programs Biomed. 27: 65-8, 1988.

The generation and selection of antibodies may be accomplished several ways. For example, one way is to purify polypeptides of interest or to synthesize the polypeptides of interest using, e.g., solid phase peptide synthesis methods well known in the art. See, e.g., Guide to Protein Purification, Murray P. Deutcher, ed., Meth. Enzymol. Vol 182 (1990); Solid Phase Peptide Synthesis, Greg B. Fields ed., Meth. Enzymol. Vol 289 (1997); Kiso et al., Chem. Pharm. Bull. (Tokyo) 38: 1192-99, 1990; Mostafavi et al., Biomed. Pept. Proteins Nucleic Acids 1: 255-60, 1995; Fujiwara et al., Chem. Pharm. Bull. (Tokyo) 44: 1326-31, 1996. The selected polypeptides may then be injected, for example, into mice or rabbits, to generate polyclonal or monoclonal antibodies. One skilled in the art will recognize that many procedures are available for the production of antibodies, for example, as described in Antibodies, A Laboratory Manual, Ed Harlow and David Lane, Cold Spring Harbor Laboratory (1988), Cold Spring Harbor, N.Y. One skilled in the art will also appreciate that binding fragments or Fab fragments which mimic antibodies can also be prepared from genetic information by various procedures (Antibody Engineering: A Practical Approach (Borrebaeck, C., ed.), 1995, Oxford University Press, Oxford; J. Immunol. 149, 3914-3920 (1992)).

In addition, numerous publications have reported the use of phage display technology to produce and screen libraries of polypeptides for binding to a selected target. See, e.g., Cwirla et al., Proc. Natl. Acad. Sci. USA 87, 6378-82, 1990; Devlin et al., Science 249, 404-6, 1990, Scott and Smith, Science 249, 386-88, 1990; and Ladner et al., U.S. Pat. No. 5,571,698. A basic concept of phage display methods is the establishment of a physical association between DNA encoding a polypeptide to be screened and the polypeptide. This physical association is provided by the phage particle, which displays a polypeptide as part of a capsid enclosing the phage genome which encodes the polypeptide. The establishment of a physical association between polypeptides and their genetic material allows simultaneous mass screening of very large numbers of phage bearing different polypeptides. Phage displaying a polypeptide with affinity to a target bind to the target and these phage are enriched by affinity screening to the target. The identity of polypeptides displayed from these phage can be determined from their respective genomes. Using these methods a polypeptide identified as having a binding affinity for a desired target can then be synthesized in bulk by conventional means. See, e.g., U.S. Pat. No. 6,057,098, which is hereby incorporated in its entirety, including all tables, figures, and claims.

The antibodies that are generated by these methods may then be selected by first screening for affinity and specificity with the purified polypeptide of interest and, if required, comparing the results to the affinity and specificity of the antibodies with polypeptides that are desired to be excluded from binding. The screening procedure can involve immobilization of the purified polypeptides in separate wells of microtiter plates. The solution containing a potential antibody or groups of antibodies is then placed into the respective microtiter wells and incubated for about 30 min to 2 h. The microtiter wells are then washed and a labeled secondary antibody (for example, an anti-mouse antibody conjugated to alkaline phosphatase if the raised antibodies are mouse antibodies) is added to the wells and incubated for about 30 min and then washed. Substrate is added to the wells and a color reaction will appear where antibody to the immobilized polypeptide(s) are present.

The antibodies so identified may then be further analyzed for affinity and specificity in the assay design selected. In the development of immunoassays for a target protein, the purified target protein acts as a standard with which to judge the sensitivity and specificity of the immunoassay using the antibodies that have been selected. Because the binding affinity of various antibodies may differ; certain antibody pairs (e.g., in sandwich assays) may interfere with one another sterically, etc., assay performance of an antibody may be a more important measure than absolute affinity and specificity of an antibody.

Those skilled in the art will recognize that many approaches can be taken in producing antibodies or binding fragments and screening and selecting for affinity and specificity for the various polypeptides, but these approaches do not change the scope of the invention.

EXAMPLES

The following examples serve to illustrate the present invention. These examples are in no way intended to limit the scope of the invention.

Example 1 Biochemical Analyses

Markers were measured using standard immunoassay techniques. These techniques involve the use of antibodies to specifically bind the analyte(s) of interest. Immunoassays were performed using TECAN Genesis RSP 200/8 or Perkin Elmer Minitrak Workstations, or using microfluidic devices manufactured at Biosite Incorporated essentially as described in WO98/43739, WO98/08606, WO98/21563, and WO93/24231. Analytes may be measured using a sandwich immunoassay or using a competitive immunoassay as appropriate, depending on the characteristics and concentration range of the analyte of interest.

The assays were calibrated using purified proteins (that is either the same as or related to the selected analyte, and that can be detected in the assay) diluted gravimetrically into EDTA plasma treated in the same manner as the sample population specimens. Endogenous levels of the analyte present in the plasma prior to addition of the purified marker protein was measured and taken into account in assigning the marker values in the calibrators. When necessary to reduce endogenous levels in the calibrators, the endogenous analyte was stripped from the plasma using standard immunoaffinity methods. Calibrators were assayed in the same manner as the sample population specimens, and the resulting data used to construct a “dose-response” curve (assay signal as a function of analyte concentration), which may be used to determine analyte concentrations from assay signals obtained from subject specimens.

Individual assays were configured to bind NGAL, and results are reported in the following examples using as ng/mL.

Example 2 Microtiter Plate-Based Biochemical Analyses

For the sandwich immunoassay in microtiter plates, a monoclonal antibody directed against a selected analyte was biotinylated using N-hydroxysuccinimide biotin (NHS-biotin) at a ratio of about 5 NHS-biotin moieties per antibody. The antibody-biotin conjugate was then added to wells of a standard avidin 384 well microtiter plate, and antibody conjugate not bound to the plate was removed. This formed the “anti-marker” in the microtiter plate. Another monoclonal antibody directed against the same analyte was conjugated to alkaline phosphatase, for example using succinimidyl 4[N-maleimidomethyl]-cyclohexane-1-carboxylate (SMCC) and N-succinimidyl 3[2-pyridyldithio]propionate (SPDP) (Pierce, Rockford, Ill.).

Biotinylated antibodies were pipetted into microtiter plate wells previously coated with avidin and incubated for 60 min. The solution containing unbound antibody was removed, and the wells washed with a wash buffer, consisting of 20 mM borate (pH 7.42) containing 150 mM NaCl, 0.1% sodium azide, and 0.02% Tween-20. The plasma samples (10 μL) containing added HAMA inhibitors were pipetted into the microtiter plate wells, and incubated for 60 min. The sample was then removed and the wells washed with a wash buffer. The antibody-alkaline phosphatase conjugate was then added to the wells and incubated for an additional 60 min, after which time, the antibody conjugate was removed and the wells washed with a wash buffer. A substrate, (AttoPhos®, Promega, Madison, Wis.) was added to the wells, and the rate of formation of the fluorescent product is related to the concentration of the analyte in the sample tested.

Example 3 Microfluidic Device-Based Biochemical Analyses

Immunoassays were performed using microfluidic devices essentially as described in Chapter 41, entitled “Near Patient Tests: Triage® Cardiac System,” in The Immunoassay Handbook, 2^(nd) ed., David Wild, ed., Nature Publishing Group, 2001.

For sandwich immunoassays, a plasma sample was added to the microfluidic device that contains all the necessary assay reagents, including HAMA inhibitors, in dried form. The plasma passed through a filter to remove particulate matter. Plasma entered a “reaction chamber” by capillary action. This reaction chamber contained fluorescent latex particle-antibody conjugates (hereafter called FETL-antibody conjugates) appropriate to an analyte of interest, and may contain FETL-antibody conjugates to several selected analytes. The FETL-antibody conjugates dissolved into the plasma to form a reaction mixture, which was held in the reaction chamber for an incubation period (about a minute) to allow the analyte(s) of interest in the plasma to bind to the antibodies. After the incubation period, the reaction mixture moved down the detection lane by capillary action. Antibodies to the analyte(s) of interest were immobilized in discrete capture zones on the surface of a “detection lane.”Analyte/antibody-FETL complexes formed in the reaction chamber were captured on an appropriate detection zone to form a sandwich complex, while unbound FETL-antibody conjugates were washed from the detection lane into a waste chamber by excess plasma. The amount of analyte/antibody-FETL complex bound on a capture zone was quantified with a fluorometer (Triage® MeterPlus, Biosite Incorporated) and was related to the amount of the selected analyte in the plasma specimen.

One skilled in the art readily appreciates that the present invention is well adapted to carry out the objects and obtain the ends and advantages mentioned, as well as those inherent therein. The examples provided herein are representative of preferred embodiments, are exemplary, and are not intended as limitations on the scope of the invention.

It will be readily apparent to a person skilled in the art that varying substitutions and modifications may be made to the invention disclosed herein without departing from the scope and spirit of the invention.

All patents and publications mentioned in the specification are indicative of the levels of those of ordinary skill in the art to which the invention pertains. All patents and publications are herein incorporated by reference to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference.

The invention illustratively described herein suitably may be practiced in the absence of any element or elements, limitation or limitations which is not specifically disclosed herein. Thus, for example, in each instance herein any of the terms “comprising”, “consisting essentially of” and “consisting of” may be replaced with either of the other two terms. The terms and expressions which have been employed are used as terms of description and not of limitation, and there is no intention that in the use of such terms and expressions of excluding any equivalents of the features shown and described or portions thereof, but it is recognized that various modifications are possible within the scope of the invention claimed. Thus, it should be understood that although the present invention has been specifically disclosed by preferred embodiments and optional features, modification and variation of the concepts herein disclosed may be resorted to by those skilled in the art, and that such modifications and variations are considered to be within the scope of this invention as defined by the appended claims.

Other embodiments are set forth within the following claims. 

We claim:
 1. A method of assigning a risk of an adverse outcome to a patient suffering from renal artery stenosis, comprising: performing an immunoassay that detects Neutophil Gelatinase-Associated Lipocalinon (NGAL) on a body fluid sample obtained from said patient, wherein said immunoassay comprises (a) contacting said body fluid sample with a solid phase comprising an antibody that detects NGAL, and (b) detecting binding to said antibody, thereby providing an NGAL assay result; comparing said NGAL assay result to a baseline NGAL result; and relating the NGAL assay result to the patient's risk of an adverse outcome by assigning an increased risk of an adverse outcome to said patient when said NGAL assay result is greater than said baseline NGAL result, or by assigning a decreased risk of an adverse outcome to said patient when said NGAL assay result is less than said baseline NGAL result.
 2. A method according to claim 1, wherein said baseline NGAL result is determined by performing an assay method that detects NGAL on a body fluid sample obtained from said patient at a time earlier than the time at which the body fluid sample used to provide said NGAL assay result was obtained.
 3. A method according to claim 1, wherein said baseline NGAL result is determined from a population of subjects suffering from renal artery stenosis, and said baseline NGAL result is selected to separate said population into a first subpopulation having an increased risk of an adverse outcome relative to a second subpopulation.
 4. A method according to claim 3, wherein said baseline NGAL result separates said first subpopulation from said second subpopulation with an odds ratio of at least 2 or more or 0.5 or less.
 5. A method according to claim 3, wherein said baseline NGAL result separates said first subpopulation from said second subpopulation with an odds ratio of at least 3 or more or 0.33 or less.
 6. A method according to claim 1, wherein said adverse outcome is mortality in the short term or worsening renal function in the short term.
 7. A method according to claim 1, wherein the body fluid sample is selected from the group consisting of urine, blood, serum, and plasma.
 8. A method according to claim 1, wherein the method further comprises determining one or more additional variables selected from the group consisting of a serum creatinine level for said patient, a creatinine clearance rate for said patient, a cystatin C level for said patient, and a glomerular filtration rate for said patient; and wherein the patient's risk of an adverse outcome is assigned based on comparing said NGAL assay result to said baseline NGAL result, and on said one or more additional variables.
 9. A method according to claim 1, wherein the method further comprises determining one or more additional variables for said patient selected from the group consisting of a urine output level for said patient, a family history of atherosclerosis, obesity, positive smoking status, prior smoking history, race, age, and diabetes mellitus; and wherein the patient's risk of an adverse outcome is assigned based on comparing said NGAL assay result to said baseline NGAL result, and on said one or more additional variables.
 10. A method according to claim 1, wherein the method further comprises: performing an assay method that detects one or more of Brain Natriuretic Peptide (BNP), NT-proBNP and proBNP on a body fluid sample obtained from said patient, thereby providing a natriuretic peptide assay result; comparing said natriuretic peptide assay result to a baseline natriuretic peptide result; and relating the natriuretic peptide assay result to the patient's risk of an adverse outcome by assigning an increased risk to said patient when said natriuretic peptide assay result is greater than said baseline natriuretic peptide result, relative to a risk assigned when said natriuretic peptide assay result is less than said baseline natriuretic peptide result, or by assigning a decreased risk to said patient when said natriuretic peptide assay result is less than said baseline natriuretic peptide result, relative to a risk assigned when said natriuretic peptide assay result is greater than said baseline natriuretic peptide result.
 11. A method according to claim 10, wherein the assay method providing the natriuretic peptide assay result and the assay method providing the NGAL assay result are performed on the same body fluid sample obtained from said patient. 